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Transducer C8-4V 989605430232Recalls & reported problems

Philips Ultrasound LLC · Class 2

All models of Transducer C8-4v (4)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Jul 3, 2025Open, Classified

    To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

    Z-2357-2025 · Root cause: Device Design · Recall details · FDA record ↗

  2. Jul 3, 2025Open, Classified

    To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

    Z-2358-2025 · Root cause: Device Design · Recall details · FDA record ↗

Other System, imaging, pulsed doppler, ultrasonic devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page